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rs180177112

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(G;T) 3 increased risk of breast cancer
(T;T) 7 Fanconi anemia, complementation group N
ReferenceGRCh38 38.1/141
Chromosome16
Position23629768
GenePALB2
is asnp
is mentioned by
dbSNPrs180177112
ebirs180177112
HLIrs180177112
Exacrs180177112
Varsomers180177112
Maprs180177112
PheGenIrs180177112
hapmaprs180177112
1000 genomesrs180177112
hgdprs180177112
ensemblrs180177112
gopubmedrs180177112
geneviewrs180177112
scholarrs180177112
googlers180177112
pharmgkbrs180177112
gwascentralrs180177112
openSNPrs180177112
23andMers180177112
23andMe allrs180177112
SNP Nexus

SNPshotrs180177112
SNPdbers180177112
MSV3drs180177112
GWAS Ctlgrs180177112
Max Magnitude7
ClinVar
Risk rs180177112(T;T)
Alt rs180177112(T;T)
Reference rs180177112(G;G)
Significance Other
Disease Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Variation info
Gene PALB2
CLNDBN Familial cancer of breast Hereditary cancer-predisposing syndrome not provided
Reversed 1
HGVS NC_000016.9:g.23641089C>A
CLNSRC PALB2 database
CLNACC RCV000114524.3, RCV000129116.2, RCV000236024.1,


[PMID 17200668OA-icon.png] PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.


[PMID 21285249OA-icon.png] Contribution of inherited mutations in the BRCA2-interacting protein PALB2 to familial breast cancer.